Surface-modified cyanide-based transition metal compounds

ABSTRACT

A system, method, and articles of manufacture for a surface-modified transition metal cyanide coordination compound (TMCCC) composition, an improved electrode including the composition, and a manufacturing method for the composition which may include multiple chelation species (Che_x). The composition, compound, device, and uses thereof according to AxMn(y-k)Mjk[Mnm(CN)(6-p-q)(NC)p(Che_I)rq]z. CHE_GROUP (Vac)(1-z).nH2O, wherein CHE_GROUP includes one or more chelation materials selected from the group consisting of (Che_I)rw, (Che_II)sv, and combinations thereof, and wherein 0&lt;j≤4, 0≤k≤0.1, 0≤(p+q)≤6, 0&lt;x≤4, 0&lt;y≤1, 0&lt;z≤1, 0&lt;w≤0.2; −3≤r≤3; 0&lt;v≤0.2; −3≤s≤3; and 0≤n≤6; wherein x+2(y−k)+jk+(m+(r+1)q−6)z+wr+vs=0.

CROSS REFERENCE TO RELATED APPLICATIONS

This Application is a Continuation of application Ser. No. 15/859,160,now U.S. Pat. No. 10,414,666, filed on Dec. 29, 2017; Application Ser.No. 15/859,160 is a Continuation of Application PCT/US16/40209 filed onJun. 29, 2016; Application PCT/US16/40209 is a Continuation ofapplication Ser. No. 14/880,010, now U.S. Pat. No. 9,359,219, filed onOct. 9, 2015; Application Ser. No. 14/880,010 is a Division ofapplication Ser. No. 14/755,607, now U.S. Pat. No. 9,299,981, filed onJun. 30, 2015; Application PCT/US16/40209 is a Continuation ofapplication Ser. No. 14/755,607, U.S. Pat. No. 9,299,981, filed on Jun.30, 2015; the contents of which are all hereby expressly incorporated byreference thereto in their entireties for all purposes.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under ARPA-E Award No.DE-AR000300 With Alveo Energy, Inc., awarded by DOE. The government hascertain rights in the invention.

FIELD OF THE INVENTION

The present invention relates generally to environmental stability ofmaterials useful in electrochemical devices, and more specifically, butnot exclusively, to compositions, articles of manufacture, and methodsfor manufacture of environmentally stabilized electrode activematerials, for example stabilization of air sensitive anode activetransition metal cyanide coordination compound (TMCCC) materials.

BACKGROUND OF THE INVENTION

The subject matter discussed in the background section should not beassumed to be prior art merely as a result of its mention in thebackground section. Similarly, a problem mentioned in the backgroundsection or associated with the subject matter of the background sectionshould not be assumed to have been previously recognized in the priorart. The subject matter in the background section merely representsdifferent approaches, which in and of themselves may also be inventions.

There is a trend in electrochemical cell design that requires adevelopment of new materials for energy storage technologies to allowfor safe, economic and energy efficient batteries. A number ofcyanide-based transition metal compounds used as cathodes have beendeveloped for organic and aqueous electrolytes. Very little work to datehas been published on cyanide-based transition metal compounds used asanodes, and more specifically, used as anode electrodes in aqueouselectrolyte batteries.

Recent developments regarding cyanide-bridged coordination polymerelectrodes for aqueous-based electrolyte batteries have revealedpromising results. However, many challenges must be have addressedbefore cyanide-based transition metal compounds may be safely,economically and used in an energy efficiently manner in an anode,especially in an anode operated in an aqueous electrolyte cell.Relatively rapid fade rates of the electrode, as well as difficulties inprocessing and handling the material in the presence of oxygen areimportant technical, economic and safety concerns.

For example, manganese hexacyanomanganate anode material is air andmoisture sensitive and thus its storage, handling, and processingrequire a controlled environment in which oxygen and moisture should beabsent. Incorporating such a material into a product, like a battery,has an important impact on a cost of fabrication of the battery andrenders the material less attractive as an anode active material despiteits potential advantages due to its electrochemical properties.

What is needed is a system, method, and articles of manufacture for animproved transition metal cyanide coordination compound (TMCCC)composition, an improved electrode including the composition, and amanufacturing method for the composition.

BRIEF SUMMARY OF THE INVENTION

Disclosed are systems, methods, and articles of manufacture for animproved transition metal cyanide coordination compound (TMCCC)composition, an improved electrode including the composition, and amanufacturing method for the composition.

The following summary of the invention is provided to facilitate anunderstanding of some of the technical features related to airstabilization of air sensitive materials, and is not intended to be afull description of the present invention. A full appreciation of thevarious aspects of the invention can be gained by taking the entirespecification, claims, drawings, and abstract as a whole. The presentinvention is applicable to other materials and processes.

Embodiments of the present invention may include a method of reacting anair sensitive material, such as a TMCCC material, that may be used in anelectrode of an electrochemical device with one or more chelatingagents. A consequence of such a method is that the resulting materialdemonstrates improved air stability without experiencing an appreciabledegradation of the desirable electrochemical and cycle life performancemetrics. These chelating agents may include an acid-containing materialthat interacts with metal ions on a surface of elements of the TMCCCmaterial. The resulting material exhibits diminished reactivity andtherefore increased stability within the ambient environment,particularly oxygen and water.

An embodiment of the present invention may include a final compositionof matter having a general formula: A_(x)M[R(CN)_(6-j)L_(j)]_(z).(Che)_(w).nH₂O, where: A is a cation; M is a metal cation; R is atransition metal cation; L is a ligand that may be substituted in theplace of a CN⁻ ligand and Che is an acid-containing chelating agent.

An embodiment of the present invention may include an electrode in anelectrochemical device, the electrode including a final composition ofmatter having a general formula: A_(x)M[R(CN)_(6-j)L_(j)]_(z).(Che)_(w).nH₂O, where: A is a cation; M is a metal cation; R is atransition metal cation; L is a ligand that may be substituted in theplace of a CN⁻ ligand and Che is an acid-containing chelating agent.

An embodiment of the present invention may include a method formanufacturing an environment-stabilized TMCCC material includingproducing a particulated TMCCC material and then washing theparticulated TMCCC material with a solution including a materialcontaining an acid group to produce a stabilized TMCCC material. Thisstabilized TMCCC material may be used in manufacturing structures usefulin electrochemical devices, such as an anode for example, with greatlydecreased concerns regarding degradation consequent to exposure toambient atmosphere.

An embodiment of the present invention may include a composition ofmatter of the formula I: A_(x)Mn_((y-k))M^(j)_(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che)^(r) _(q)]_(z). (Che)^(r)_(w)(Vac)_((1-z)).nH₂O (Formula I), including surface-modifiedcyanide-bridged coordination polymers having well faceted cubic crystalstructures with crystal size of more than 1 micron and having diminishedsurface reactivity exhibit improved air stability.

A method for manufacturing an environment-stabilized TMCCC material,including a) synthesizing a particulated TMCCC material from a precursorsalt, said precursor salt including a transition metal and a firstchelation species (Che_I); and thereafter b) combining the particulatedTMCCC material with a solution including a second chelation species(Che_II) to produce a stabilized TMCCC, said second chelation speciesincluding one or more chemical species selected from the group includinga first material including said first chelation species, a secondmaterial excluding said first chelation species, and combinationsthereof;

-   -   wherein said stabilized TMCCC material includes:    -   at least one composition represented by Formula II:

A_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che_I)^(r)_(q)]_(z).CHE_GROUP (Vac)_((1-z)) .nH₂O,  (Formula II):

wherein CHE_GROUP includes one or more chelation materials selected fromthe group consisting of (Che_I)^(r) _(w), (Che_II)^(s) _(v), andcombinations thereofwherein, in Formula II, each A is an independently selected alkali metalLi, Na, or K; and each dopant M may optionally be at least oneindependently selected alkaline earth metal Mg or Ca, post-transitionmetal Al, Ga, In, Sn, or Pb, or transition metal Sc, Ti, V, Cr, Fe, Co,Ni, Cu, Zn, Pd, Ag, or Cd having an average valence j; and Cherepresents an acid chelating agent which includes ligand binding atomsthat form one or more covalent linkages with Mn or with Mn and M; andwherein 0<j≤4, 0≤k≤0.1, 0≤(p+q)≤6, 0<x≤4, 0<y≤1, 0<z≤1, 0<w≤0.2; −3≤r≤3;0<v≤0.2; −3≤s≤3; and 0≤n≤6;wherein x+2(y−k)+jk+(m+(r+1)q−6)z+wr+vs=0; andwherein Formula I includes one or moreMn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes each including an Mnatom, and wherein p is an average number of NC groups found in said oneor more Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; and whereinq is an average number of Che_I groups found in said one or moreMn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; andwherein m is an average valence of said Mn atoms found in said one ormore Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes;wherein (Vac) identifies a Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q)vacancy;wherein CN identifies a cyano group; andwherein NC identifies an isocyano group.

An embodiment of the present invention may include two chelation species(Che_I and Che_II).—for example Che_I is present during a synthesis, soit can be more easily substituted into the hexacyano complexes inquantity q. Che_II, on the other hand, may only be present after thesynthesis during a washing step. The specification evidences that Che_IImay displace some Che_1 on the surface of the particles (quantity w ofChe_I replaced by quantity v of Che_II). It is not believed that it islikely that Che_II could partially or fully displace Che_I in thecomplexes in quantity q.

An embodiment may include different related products represented byA_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che_I)^(r)_(q)]_(z). CHE_GROUP (Vac)_((1-z)).nH₂O wherein the Che_I species is the“in-structure” chelation species present during synthesis and theCHE_GROUP represents chelation species on surface and may include Che_Iand/or Che_II.

An embodiment of the present invention may include a method, product,composition allowing for multiple chelation species in Formula I,including: a) synthesis with Che_I; b) isolation to remove product fromsynthesis solution; c) washing the isolated product from b) with asolution containing no chelating agents (removes any excess Che_I) whichproduces a product 1 wherein CHE_GROUP includes only Che_I; d) washingthis product 1 with a solution containing Che_II which results inCHE_GROUP at this stage including some or all of Che_II; and e) a finalisolation (e.g., filtration) to remove excess Che_II solution, resultingin a product 2 different from product 1 in that CHE_GROUP has Che_IIreplacing some or all of Che_I on the surface. A variation of this mayinclude a step f) after step a) to add Che_II to the synthesis solutionand then followed by a step g) to isolate/wash with a solutioncontaining no chelating agents (similar to step c) which results,broadly, in product 2 with some or all surface Che_I replaced by Che_II.

Embodiments of surface modified cyanide-bridged coordination polymers ofthe present invention exhibit very good air stability. In someembodiments, a surface oxidation of particles of these materials, uponexposure to air, was negligible even after 60 hours. Comparisons betweenexposed and unexposed materials to air shows that there is no differencebetween their electrochemical performances and that there is an order ofmagnitude improvement of their fade capacity loss compared to othercyanide-based transition metal compounds.

From safety and economic point of view, the ease of preparation andimproved air stability of theses novel materials makes them veryattractive candidate in the family of cyanide-bridged coordinationpolymer-based anodes for electrochemical devices, such as batterytechnology for example.

These materials can be used in electrodes for electrochemical energystorage devices such as batteries. These batteries can be used forapplications including stationary storage, vehicles, and portableelectronics. These materials can also be used as electrochromicelectrodes in electrochromic devices.

Any of the embodiments described herein may be used alone or togetherwith one another in any combination. Inventions encompassed within thisspecification may also include embodiments that are only partiallymentioned or alluded to or are not mentioned or alluded to at all inthis brief summary or in the abstract. Although various embodiments ofthe invention may have been motivated by various deficiencies with theprior art, which may be discussed or alluded to in one or more places inthe specification, the embodiments of the invention do not necessarilyaddress any of these deficiencies. In other words, different embodimentsof the invention may address different deficiencies that may bediscussed in the specification. Some embodiments may only partiallyaddress some deficiencies or just one deficiency that may be discussedin the specification, and some embodiments may not address any of thesedeficiencies.

Other features, benefits, and advantages of the present invention willbe apparent upon a review of the present disclosure, including thespecification, drawings, and claims.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying figures, in which like reference numerals refer toidentical or functionally-similar elements throughout the separate viewsand which are incorporated in and form a part of the specification,further illustrate the present invention and, together with the detaileddescription of the invention, serve to explain the principles of thepresent invention.

FIG. 1a -FIG. 1d illustrate a set of scanning electron microscopy (SEM)images of oxalic acid surface-modified materials at different exposuretime to air;

FIG. 1a illustrates an SEM image of an oxalic acid surface-modifiedTMCCC material after exposure to air for 0 hours;

FIG. 1b illustrates an SEM image of an oxalic acid surface-modifiedTMCCC material after exposure to air for 2 hours;

FIG. 1c illustrates an SEM image of an oxalic acid surface-modifiedTMCCC material after exposure to air for 10 hours; and

FIG. 1d illustrates an SEM image of an oxalic acid surface-modifiedTMCCC material after exposure to air for 60 hours;

FIG. 2a -FIG. 2d illustrate a set of scanning electron microscopy (SEM)images of surface-modified versus surface-unmodified TMCCC materialsexposed to air;

FIG. 2a illustrates an SEM image of a surface-unmodified TMCCC materialafter exposure to air for 2 hours;

FIG. 2b illustrates an SEM image of a surface-modified TMCCC material(with citric acid) after exposure to air for 2 hours;

FIG. 2c illustrates an SEM image of a surface-modified TMCCC material(with malic acid) after exposure to air for 10 hours; and

FIG. 2d illustrates an SEM image of a surface-modified TMCCC material(with sodium glycinate) after exposure to air for 10 hours; and

FIG. 3 illustrates a cycle life of electrodes made of surface-modifiedTMCCC materials and surface-unmodified TMCCC materials exposed to air;

FIG. 4 illustrates a cycle life of oxalic acid surface-modified TMCCCmaterials and surface-unmodified TMCCC materials after 2 hours exposureto air; and

FIG. 5 illustrates a representative secondary electrochemical cellschematic having one or more surface-modified TMCCC electrodes disposedin contact with an electrolyte.

DETAILED DESCRIPTION OF THE INVENTION

Embodiments of the present invention provide systems, methods, andarticles of manufacture for an improved transition metal cyanidecoordination compound (TMCCC) composition, an improved electrodeincluding the composition, and a manufacturing method for thecomposition. The following description is presented to enable one ofordinary skill in the art to make and use the invention and is providedin the context of a patent application and its requirements.

Various modifications to the preferred embodiment and the genericprinciples and features described herein will be readily apparent tothose skilled in the art. Thus, the present invention is not intended tobe limited to the embodiment shown but is to be accorded the widestscope consistent with the principles and features described herein.

Definitions

Unless otherwise defined, all terms (including technical and scientificterms) used herein have the same meaning as commonly understood by oneof ordinary skill in the art to which this general inventive conceptbelongs. It will be further understood that terms, such as those definedin commonly used dictionaries, should be interpreted as having a meaningthat is consistent with their meaning in the context of the relevant artand the present disclosure, and will not be interpreted in an idealizedor overly formal sense unless expressly so defined herein.

The following definitions apply to some of the aspects described withrespect to some embodiments of the invention. These definitions maylikewise be expanded upon herein.

As used herein, the term “or” includes “and/or” and the term “and/or”includes any and all combinations of one or more of the associatedlisted items. Expressions such as “at least one of,” when preceding alist of elements, modify the entire list of elements and do not modifythe individual elements of the list.

As used herein, the singular terms “a,” “an,” and “the” include pluralreferents unless the context clearly dictates otherwise. Thus, forexample, reference to an object can include multiple objects unless thecontext clearly dictates otherwise.

Also, as used in the description herein and throughout the claims thatfollow, the meaning of “in” includes “in” and “on” unless the contextclearly dictates otherwise. It will be understood that when an elementis referred to as being “on” another element, it can be directly on theother element or intervening elements may be present therebetween. Incontrast, when an element is referred to as being “directly on” anotherelement, there are no intervening elements present.

As used herein, the term “set” refers to a collection of one or moreobjects. Thus, for example, a set of objects can include a single objector multiple objects. Objects of a set also can be referred to as membersof the set. Objects of a set can be the same or different. In someinstances, objects of a set can share one or more common properties.

As used herein, the term “adjacent” refers to being near or adjoining.Adjacent objects can be spaced apart from one another or can be inactual or direct contact with one another. In some instances, adjacentobjects can be coupled to one another or can be formed integrally withone another.

As used herein, the terms “connect,” “connected,” and “connecting” referto a direct attachment or link. Connected objects have no or nosubstantial intermediary object or set of objects, as the contextindicates.

As used herein, the terms “couple,” “coupled,” and “coupling” refer toan operational connection or linking. Coupled objects can be directlyconnected to one another or can be indirectly connected to one another,such as via an intermediary set of objects.

As used herein, the terms “substantially” and “substantial” refer to aconsiderable degree or extent. When used in conjunction with an event orcircumstance, the terms can refer to instances in which the event orcircumstance occurs precisely as well as instances in which the event orcircumstance occurs to a close approximation, such as accounting fortypical tolerance levels or variability of the embodiments describedherein.

The use of the term “about” applies to all numeric values, whether ornot explicitly indicated. This term generally refers to a range ofnumbers that one of ordinary skill in the art would consider as areasonable amount of deviation to the recited numeric values (i.e.,having the equivalent function or result). For example, this term can beconstrued as including a deviation of ±10 percent of the given numericvalue provided such a deviation does not alter the end function orresult of the value. Therefore, a value of about 1% can be construed tobe a range from 0.9% to 1.1%.

As used herein, the terms “optional” and “optionally” mean that thesubsequently described event or circumstance may or may not occur andthat the description includes instances where the event or circumstanceoccurs and instances in which it does not.

As used herein, the term “size” refers to a characteristic dimension ofan object. Thus, for example, a size of an object that is spherical canrefer to a diameter of the object. In the case of an object that isnon-spherical, a size of the non-spherical object can refer to adiameter of a corresponding spherical object, where the correspondingspherical object exhibits or has a particular set of derivable ormeasurable properties that are substantially the same as those of thenon-spherical object. Thus, for example, a size of a non-sphericalobject can refer to a diameter of a corresponding spherical object thatexhibits light scattering or other properties that are substantially thesame as those of the non-spherical object. Alternatively, or inconjunction, a size of a non-spherical object can refer to an average ofvarious orthogonal dimensions of the object. Thus, for example, a sizeof an object that is a spheroidal can refer to an average of a majoraxis and a minor axis of the object. When referring to a set of objectsas having a particular size, it is contemplated that the objects canhave a distribution of sizes around the particular size. Thus, as usedherein, a size of a set of objects can refer to a typical size of adistribution of sizes, such as an average size, a median size, or a peaksize.

FIG. 1a -FIG. 1d illustrate a set of scanning electron microscopy (SEM)images of oxalic acid surface-modified materials at different exposuretime to air; FIG. 1a illustrates an SEM image of an oxalic acidsurface-modified TMCCC material after exposure to air for 0 hours; FIG.1b illustrates an SEM image of an oxalic acid surface-modified TMCCCmaterial after exposure to air for 2 hours; FIG. 1c illustrates an SEMimage of an oxalic acid surface-modified TMCCC material after exposureto air for 10 hours; and FIG. 1d illustrates an SEM image of an oxalicacid surface-modified TMCCC material after exposure to air for 60 hours.

FIG. 2a -FIG. 2d illustrate a set of scanning electron microscopy (SEM)images of surface-modified versus surface-unmodified TMCCC materialsexposed to air; FIG. 2a illustrates an SEM image of a surface-unmodifiedTMCCC material after exposure to air for 2 hours; FIG. 2b illustrates anSEM image of a surface-modified TMCCC material (with citric acid) afterexposure to air for 2 hours; FIG. 2c illustrates an SEM image of asurface-modified TMCCC material (with malic acid) after exposure to airfor 10 hours; and FIG. 2d illustrates an SEM image of a surface-modifiedTMCCC material (with sodium glycinate) after exposure to air for 10hours.

FIG. 3 illustrates a cycle life of electrodes made of surface-modifiedTMCCC materials and surface-unmodified TMCCC materials exposed to air.

FIG. 4 illustrates a cycle life of oxalic acid surface-modified TMCCCmaterials and surface-unmodified TMCCC materials after 2 hours exposureto air.

Some embodiments of the present invention may be intended to overcomeambient atmosphere stability problems and may include surface-modifiedcyanide-bridged coordination polymers anodes for use in batteries, andmore specifically, to electrodes including anodes having improved airstability, fade rate and excellent energy efficiency.

It is known that cyanide-bridged coordination polymers are capable ofstoring ions exchanged in electrochemical processes for the storage andextraction of electrical energy. Ion insertion/extraction accompanied byoxidation-reduction of these coordination polymers make these materialsgood candidates as electrode compounds in rechargeable batteries.

The ion storage efficiency of the cyanide-bridged coordination polymersis related to its structure and, in theory, the Perovskite-typestructure A₂M^(II)[M′^(II)(CN)₆] (where A is an alkali cation and M andM′ are transition metals) is the structure which provides the highestelectrode efficiency. However, it has been demonstrated that preparationof Perovskite-type structural framework is not a trivial process andthis is specifically true for air sensitive alkali cation salts ofManganese (II) hexacayanomanganate compounds that may be included inembodiments of the present invention.

A cyanide-bridged coordination polymer embodiment of the presentinvention may be represented by the formula I:

A_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che)^(r)_(q)]_(z).(Che)^(r) _(w)(Vac)_((i-z)) .nH₂O  (Formula I)

wherein, in Formula I, each A is an independently selected alkali metalLi, Na, or K; and each dopant M may optionally be at least oneindependently selected alkaline earth metal Mg or Ca, post-transitionmetal Al, Ga, In, Sn, or Pb, or transition metal Sc, Ti, V, Cr, Fe, Co,Ni, Cu, Zn, Pd, Ag, or Cd having an average valence j; and Cherepresents an organic acid chelating agent which possesses ligandbinding atoms that form one or more covalent linkages with Mn or with Mnand M, and wherein 0<j≤4, 0≤k≤0.1, 0≤(p+q)<6, 0<x≤4, 0<y≤1, 0<z≤1,0<w≤0.2 and 0≤n≤6; −3≤r≤3; wherein x+2(y−k)+jk+(m+(r+1)q−6)z+wr=0; andwherein Formula I includes one or more Mn(CN)_((6-p-q))(NC)_(p)(Che)^(r)_(q) complexes each including an Mn atom, and wherein p is an averagenumber of NC groups found in said one or moreMn(CN)_((6-p-q))(NC)_(p)(Che)^(r) _(q) complexes; and wherein q is anaverage number of Che groups found in said one or moreMn(CN)_((6-p-q))(NC)_(p)(Che)^(r) _(q) complexes; and wherein m is anaverage valence of said Mn atoms found in said one or moreMn(CN)_((6-p-q))(NC)_(p)(Che)^(r) _(q) complexes; and wherein (Vac)identifies a Mn(CN)_((6-p-q))(NC)_(p)(Che)^(r) _(q) vacancy.

Some embodiments of the cyanide-bridged coordination polymers of thepresent invention may have a very well faceted cubic crystal structureswith crystal size of more than 1 micron. A chemical treatment of theseparticles, by simple and straightforward ligand exchange procedures bywhich the metal ions on the surface of the particles are bound by astrong chelating agent, provide materials with diminished surfacereactivity and thus improved air stability.

The enhanced air stability of the materials of some embodiments of thepresent invention and the possibility of handling and processing them inair rather than in a controlled inert atmosphere makes these materialsvery attractive as electrode components in rechargeable batteries.

Processes for preparing these products are described in examples 4-15 ofthe experimental section below. A preferred method of preparationcorresponds to a molar ratio of sodium cyanide to manganese (II) salt ofmore than 3 to 1. A most preferred molar ratio of sodium cyanide tomanganese (II) salt is ranged from 3.0 to 1.0 to 3.3 to 1.0. A preferredmanganese (II) salt is manganese (II) acetate hydrates. Preferredsolvents include ethanol, methanol, and water, and their mixtures. Amost preferred solvent is water. A temperature at which the reaction iscarried out is ranged from 5 degrees Celsius to 40 degrees Celsius. Apreferred temperature range is between 5 to 20 degrees Celsius. Apreferred addition sequence is an addition of sodium cyanide solution tomanganese (II) salt solution. An addition rate is preferred to bebetween approximately 1 min to 1 hour. A preferred addition rate is fastaddition between 1 min to 20 min. Sodium cyanide is used as solid or insolution in water from concentration between 1.0 to 45.0 wt/wt %. Apreferred concentration of sodium cyanide solution is between 15 to 20wt/wt % in water. A preferred concentration of manganese (II) acetatehydrate in water is between 5 to 30 wt/wt %. A more preferred manganese(II) acetate hydrate in water is between 15 to 20 wt/wt %.

A composition including an embodiment of the present invention maycorrespond to a composition used for preparation of an anode electrode.This composition corresponds to a slurry or ink applied on a currentcollector. A composition corresponds to a mixture of an embodiment ofthe present invention, a binder, an electrical conductive material,additives and a solvent. The binder may be one or more componentsselected from the group consisting of avinylfluoride/hexafluoropropylene copolymer, polyvinylidenefluoride(PVDF), polyacrylonitrile, polymethylmethacrylate,polytetrafluoroethylene, a mixture thereof, and styrene butadienerubber-based polymer. The electrical conductive material may be selectedfrom a crystalline carbon, an amorphous carbon, or a mixture thereof.The conductive material may be selected from acetylene black, ketjenblack, natural graphite, artificial graphite, carbon black, carbonfiber, carbon nanotubes and graphene.

A solvent may be selected from solvents such as N-methylpyrrolidinone,N,N-dimethyformamide, dimethyl acetamide and dimethylsufoxide. Thepreferred solvent is N-methylpyrrolidinone.

Electrodes Preparation:

Manganese (II) hexacyanomanganate (II) salt selected from one of theexamples disclosed herein was thoroughly mixed with carbon black (Timcalsuper C65) by grinding in a mortar pestle. A resulting grey powder wasthen mixed with a solution of polyvinylidene fluoride (Kynar HSV900) inN-methyl-2-pyrolidinone to produce a slurry. A mass ratio of activematerial, carbon black and polyvinylidene fluoride was 80:10:10. A thinlayer of the thus obtained slurry was coated on a carbon cloth currentcollector to provide an electrode (intended to be an anode electrode)that was dried under vacuum. The resulting anode electrode is usedwithout further treatment in electrochemical cell setups including thefollowing air stability tests.

Air Stability Tests:

The products 1a-15a of the experimental section below were exposed toair for 2.0 hr to 60.0 hr and the resulting exposed powders were used inelectrodes preparation as described above. The electrochemicalproperties of these materials after exposure to air were compared totheir corresponding unexposed materials.

Analysis by Scanning Electron Microscopy (SEM) provided some evidenceabout the extent of surface protection of the particles againstoxidation and decomposition. (See FIG. 1a -FIG. 1d and FIG. 2a -FIG. 2d). FIG. 1a -FIG. 1d illustrate SEM images of oxalic acidsurface-modified materials at different exposure time to air. These SEMimages clearly show that these particles are pristine with no evidenceof surface oxidation even after 60 hours exposure time to air.

FIG. 2a illustrates SEM images of surface-unmodified material exposed toair for 2.0 hours with clear evidence of surface oxidation of particlesresulting in formation of white spots and roughening of the surface. Incontrast, FIG. 2b -FIG. 2d illustrate surface modified particlesresulting from citric acid, malic acid and sodium glycinate treatments,respectively, show no evidence of surface oxidation or decompositionafter 2 hours (FIG. 2b ) and 10 hours (FIG. 2c and FIG. 2d ) of exposureto air.

FIG. 3 illustrates a cycle life of electrodes made of surface-modifiedand surface-unmodified materials exposed to air. Comparisons betweensurface-modified and surface-unmodified materials shows that all thesurface-modified materials retain their capacity after more than 250cycles whereas the surface-unmodified material shows a noticeablecapacity loss after 250 cycles.

FIG. 4 illustrates a cycle life of oxalic acid surface-modifiedmaterials and surface-unmodified materials after 2 hours exposure toair. Comparisons between oxalic acid surface-modified andsurface-unmodified materials shows that surface-modified materialsretain their capacity after 200 cycles whereas the surface-unmodifiedmaterial shows a noticeable capacity loss after 200 cycles.

Table I shows a significant oxidation and capacity loss of surfaceunmodified materials after 2.0 hours exposure to air.

TABLE I Electrochemical Analysis of Surface-Unmodified Materials Exposedto Air for 2 Hours Initial Open Cycle 5 Specific Circuit VoltageCapacity (V vs. Ag/AgCl) (mAh/g) 0 Hours 2 Hours 0 Hours 2 Hours air Airair Air Product # Exposure Exposure Exposure Exposure 1a. −0.310 −0.19467.88 51.73 2a. −0.319 −0.157 64.52 31.09 3a. −0.260 −0.218 66.00 55.37

Table II shows a result of an electrochemical analysis ofsurface-modified materials after exposure to air and the evidence ofprotection of their surfaces against oxidation and remarkable retentionof their specific capacities.

TABLE II Electrochemical Analysis of Surface-Modified Materials AfterExposure to Air Initial Open Circuit Voltage Cycle 5 Specific Capacity(V vs. Ag/AgCl) (mA/g) 0 Hours 2 Hours 10 Hours 0 Hours 2 Hours 10 HoursAir Air Air Air Air Air Product # Exposure Exposure Exposure ExposureExposure Exposure 4a. −0.283 −0.281 62.51 64.82 5a. −0.352 −0.257 −0.23064.91 67.34 63.12 6a. −0.348 −0.251 −0.223 65.61 67.88 61.26 7a. −0.327−0.253 −0.198 62.21 62.20 59.70 8a. −0.360 −0.240 −0.222 66.75 59.1760.32 9a. −0.328 −0.230 67.72 63.96 10a.  −0.310 −0.232 69.42 63.5111a.  −0.353 −0.233 66.77 61.80 12a.  −0.285 −0.223 66.26 62.03 13a. −0.261 −0.257 −0.237 68.03 66.95 65.57 14a.  −0.292 −0.287 −0.239 71.6766.05 65.03

Table III shows that oxalic acid surface modification of the particlesresulted in remarkable inhibition of surface oxidation of the particleswith significant retention of specific capacity.

TABLE III Electrochemical Analysis of Oxalic Acid Surface- ModifiedMaterial After Exposure to Air Product 4a Time Initial Open Cycle 5Specific Exposure Circuit Voltage Capacity (mins) (V vs. Ag/AgCl) (mA/g)120 −0.281 64.82 1800 −0.248 60.69 2880 −0.241 63.89 3600 −0.223 64.09

FIG. 5 illustrates a representative secondary electrochemical cell 500schematic having one or more surface-modified TMCCC electrodes disposedin contact with an electrolyte as described herein. Cell 500 includes anegative electrode 505, a positive electrode 510 and an electrolyte 515electrically communicated to the electrodes. One or both of negativeelectrode 505 and positive electrode 510 include TMCCC as anelectrochemically active material. A negative current collector 520including an electrically conductive material conducts electrons betweennegative electrode 505 and a first cell terminal (not shown). A positivecurrent collector 525 including an electrically conductive materialconducts electrons between positive electrode 510 and a second cellterminal (not shown). These current collectors permit cell 500 toprovide electrical current to an external circuit or to receiveelectrical current/energy from an external circuit during recharging. Inan actual implementation, all components of cell 500 are appropriatelyenclosed, such as within a protective housing with current collectorsexternally accessible. There are many different options for the formatand arrangement of the components across a wide range of actualimplementations, including aggregation of multiple cells into a batteryamong other uses and applications.

A method for manufacturing an environment-stabilized TMCCC material,including a) synthesizing a particulated TMCCC material from a precursorsalt, said precursor salt including a transition metal and a firstchelation species (Che_I); and thereafter b) combining the particulatedTMCCC material with a solution including a second chelation species(Che_II) to produce a stabilized TMCCC, said second chelation speciesincluding one or more chemical species selected from the group includinga first material including said first chelation species, a secondmaterial excluding said first chelation species, and combinationsthereof;

wherein said stabilized TMCCC material includes:at least one composition represented by Formula II:

A_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che_I)^(r)_(q)]_(z).CHE_GROUP (Vac)_((1-z)) .nH₂O,  (Formula II):

wherein CHE_GROUP includes one or more chelation materials selected fromthe group consisting of (Che_I)^(r) _(w), (Che_II)^(s) _(v), andcombinations thereofwherein, in Formula II, each A is an independently selected alkali metalLi, Na, or K; and each dopant M may optionally be at least oneindependently selected alkaline earth metal Mg or Ca, post-transitionmetal Al, Ga, In, Sn, or Pb, or transition metal Sc, Ti, V, Cr, Fe, Co,Ni, Cu, Zn, Pd, Ag, or Cd having an average valence j; and Cherepresents an acid chelating agent which includes ligand binding atomsthat form one or more covalent linkages with Mn or with Mn and M; andwherein 0<j≤4, 0≤k≤0.1, 0≤(p+q)≤6, 0<x≤4, 0<y≤1, 0<z≤1, 0<w≤0.2; −3≤r≤3;0<v≤0.2; −3≤s≤3; and 0≤n≤6;wherein x+2(y−k)+jk+(m+(r+1)q−6)z+wr+vs=0; andwherein Formula II includes one or moreMn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes each including an Mnatom, and wherein p is an average number of NC groups found in said oneor more Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; and whereinq is an average number of Che_I groups found in said one or moreMn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; andwherein m is an average valence of said Mn atoms found in said one ormore Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes;wherein (Vac) identifies a Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q)vacancy;wherein CN identifies a cyano group; andwherein NC identifies an isocyano group.

An embodiment of the present invention may include two chelation species(Che_I and Che_II).—for example Che_I is present during a synthesis, soit can be more easily substituted into the hexacyano complexes inquantity q. Che_II, on the other hand, may only be present after thesynthesis during a washing step. The specification evidences that Che_IImay displace some Che 1 on the surface of the particles (quantity w ofChe_I replaced by quantity v of Che_II). It is not believed that it islikely that Che_II could partially or fully displace Che_I in thecomplexes in quantity q.

An embodiment may include different related products represented byA_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che_I)^(r)_(q)]_(z). CHE_GROUP (Vac)_((1-z)).nH₂O wherein the Che_I species is the“in-structure” chelation species present during synthesis and theCHE_GROUP represents one or more chelation species on a surface and mayinclude Che_I and/or Che_II.

An embodiment of the present invention may include a method, product,composition allowing for multiple chelation species in Formula II,including: a) synthesis with Che_I; b) isolation to remove product fromsynthesis solution; c) washing the isolated product from b) with asolution containing no chelating agents (removes any excess Che_I) whichproduces a product 1 wherein CHE_GROUP includes only Che_I; d) washingthis product 1 with a solution containing Che_II which results inCHE_GROUP at this stage including some or all of Che_II; and e) a finalisolation (e.g., filtration) to remove excess Che_II solution, resultingin a product 2 different from product 1 in that CHE_GROUP has Che_IIreplacing some or all of Che_I on the surface. A variation of this mayinclude a step f) after step a) to add Che_II to the synthesis solutionand then followed by a step g) to isolate/wash with a solutioncontaining no chelating agents (similar to step c) which results,broadly, in product 2 with some or all surface Che_I replaced by Che_II.In this regard, formula II is a generalized representation of formula Ithat allows for introduction of a second different chelation speciesinto the formation process after synthesis using a first chelationspecies. Without post-synthesis introduction of Che_II, formula IIidentifies the same resulting product as formula I.

EXPERIMENTAL SECTION Example 1: (Product 1a)

To a stirred solution of manganese chloride tetrahydrate (23.75 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (90 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaerated water(50 ml), rinsed with deaerated methanol (200 ml) and dried under vacuumto give 19.7 g of a blue powder.

Example 2: (Product 2a)

To a stirred solution of manganese sulfate monohydrate (20.28 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaerated water(50 ml), rinsed with deaerated methanol (200 ml) and dried under vacuumto give 20.0 g of a blue powder.

Example 3: (Product 3a)

To a stirred solution of manganese acetate tetrahydrate (29.4 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (250 ml) and dried under vacuum to give 20.0 g of a bluepowder.

Example 4—Surface Functionalization of Particles: (Product 4a)

To a stirred solution of manganese acetate tetrahydrate (29.4 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of oxalic acid in deaeratedmethanol (20 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 20.0 g of agrey-blue powder.

Example 5—Surface Functionalization of Particles: (Product 5a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of citric acid in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 9.8 g of a grey-bluepowder.

Example 6—Surface Functionalization of Particles: (Product 6a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of tartaric acid in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 9.9 g of a grey-bluepowder.

Example 7—Surface Functionalization of Particles: (Product 7a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of glycolic acid in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 9.8 g of a grey-bluepowder.

Example 8—Surface Functionalization of Particles: (Product 8a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of succinic acid in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 10.0 g of agrey-blue powder.

Example 9—Surface Functionalization of Particles: (Product 9a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of malic acid in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 9.8 g of a grey-bluepowder.

Example 10—Surface Functionalization of Particles: (Product 10a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of lactic acid (88%) in deaeratedmethanol (2.5 wt/wt %, 100 ml) followed by deaerated methanol (150 ml).The resulting powder was dried under vacuum to give 9.7 g of a grey-bluepowder.

Example 11—Surface Functionalization of Particles: (Product 11a)

To a stirred solution of manganese acetate tetrahydrate (29.4 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with a solution ofacetic acid in deaerated methanol (30 V/V %, 50 ml) followed bydeaerated methanol (150 ml). The resulting powder was dried under vacuumto give 20.0 g of a blue powder.

Example 12—Surface Functionalization of Particles: (Product 12a)

To a stirred solution of manganese acetate tetrahydrate (29.4 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then filtered over a 0.45micron filter. The resulting blue powder was washed with deaeratedmethanol (50 ml) then with a solution of HEDP (hydroxyethane dimethylenephosphonic acid) in deaerated methanol (5.0 wt/wt %, 50 ml) followed bydeaerated methanol (150 ml). The resulting powder was dried under vacuumto give 20.0 g of a blue powder.

Example 13—Surface Functionalization of Particles: (Product 13a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an hour and then sodium glycinate (1.0 g) wasadded in powder and the mixture was stirred for an additional 10 min.The mixture was then filtered over a 0.45 micron filter. The resultingblue powder was washed with deaerated methanol (150 ml) and then driedunder vacuum to give 9.8 g of a grey-blue powder.

Example 14—Surface Functionalization of Particles: (Product 14a)

To a stirred solution of manganese acetate tetrahydrate (29.4 g, 120.0mmoles) in deaerated water (120 g), a solution of sodium cyanide (19.2g, 392.0 mmoles) in deaerated water (100 g) was rapidly added over 1.0min. under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an additional hour and then EDTA (ethylenediamine tetra-acetic acid) tetrasodium salt (2.0 g) was added in powderand the mixture was stirred for an additional 10 min. The mixture wasthen filtered over a 0.45 micron filter. The resulting blue powder waswashed with deaerated methanol (250 ml) and then dried under vacuum togive 20.0 g of a blue powder.

Example 15—Surface Functionalization of Particles: (Product 15a)

To a stirred solution of manganese acetate tetrahydrate (14.7 g, 60.0mmoles) in deaerated water (60 g), a solution of sodium cyanide (9.6 g,196.0 mmoles) in deaerated water (50 g) was rapidly added over 1.0 min.under inert atmosphere of nitrogen (oxygen <0.1 ppm). The resultingmixture was stirred for an hour and then sodium oxalate (4.0 g) wasadded in powder and the mixture was stirred for an additional 10 min.The mixture was then filtered over a 0.45 micron filter. The resultingblue powder was washed with deaerated methanol (150 ml) and then driedunder vacuum to give 10.0 g of a grey-blue powder.

The systems, methods, compositions, materials, and articles ofmanufacture above have been described in general terms as an aid tounderstanding details of preferred embodiments of the present invention.In the description herein, numerous specific details are provided, suchas examples of components and/or methods, to provide a thoroughunderstanding of embodiments of the present invention. Some features andbenefits of the present invention are realized in such modes and are notrequired in every case. One skilled in the relevant art will recognize,however, that an embodiment of the invention can be practiced withoutone or more of the specific details, or with other apparatus, systems,assemblies, methods, components, materials, parts, and/or the like. Inother instances, well-known structures, materials, or operations are notspecifically shown or described in detail to avoid obscuring aspects ofembodiments of the present invention.

Reference throughout this specification to “one embodiment”, “anembodiment”, or “a specific embodiment” means that a particular feature,structure, or characteristic described in connection with the embodimentis included in at least one embodiment of the present invention and notnecessarily in all embodiments. Thus, respective appearances of thephrases “in one embodiment”, “in an embodiment”, or “in a specificembodiment” in various places throughout this specification are notnecessarily referring to the same embodiment. Furthermore, theparticular features, structures, or characteristics of any specificembodiment of the present invention may be combined in any suitablemanner with one or more other embodiments. It is to be understood thatother variations and modifications of the embodiments of the presentinvention described and illustrated herein are possible in light of theteachings herein and are to be considered as part of the spirit andscope of the present invention.

It will also be appreciated that one or more of the elements depicted inthe drawings/figures can also be implemented in a more separated orintegrated manner, or even removed or rendered as inoperable in certaincases, as is useful in accordance with a particular application.

Additionally, any signal arrows in the drawings/Figures should beconsidered only as exemplary, and not limiting, unless otherwisespecifically noted. Combinations of components or steps will also beconsidered as being noted, where terminology is foreseen as renderingthe ability to separate or combine is unclear.

The foregoing description of illustrated embodiments of the presentinvention, including what is described in the Abstract, is not intendedto be exhaustive or to limit the invention to the precise formsdisclosed herein. While specific embodiments of, and examples for, theinvention are described herein for illustrative purposes only, variousequivalent modifications are possible within the spirit and scope of thepresent invention, as those skilled in the relevant art will recognizeand appreciate. As indicated, these modifications may be made to thepresent invention in light of the foregoing description of illustratedembodiments of the present invention and are to be included within thespirit and scope of the present invention.

Thus, while the present invention has been described herein withreference to particular embodiments thereof, a latitude of modification,various changes and substitutions are intended in the foregoingdisclosures, and it will be appreciated that in some instances somefeatures of embodiments of the invention will be employed without acorresponding use of other features without departing from the scope andspirit of the invention as set forth. Therefore, many modifications maybe made to adapt a particular situation or material to the essentialscope and spirit of the present invention. It is intended that theinvention not be limited to the particular terms used in followingclaims and/or to the particular embodiment disclosed as the best modecontemplated for carrying out this invention, but that the inventionwill include any and all embodiments and equivalents falling within thescope of the appended claims. Thus, the scope of the invention is to bedetermined solely by the appended claims.

What is claimed as new and desired to be protected by Letters Patent ofthe United States is:
 1. A material, comprising: at least onecomposition represented by Formula II:A_(x)Mn_((y-k))M^(j) _(k)[Mn^(m)(CN)_((6-p-q))(NC)_(p)(Che_I)^(r)_(q)]_(z).CHE_GROUP (Vac)_((i-z)) .nH₂O,  (Formula II): whereinCHE_GROUP includes one or more chelation materials selected from thegroup consisting of (Che_I)^(r) _(w), (Che_II)^(s) _(v), wherein Che_Iincludes a first chelation species and Che_II includes a secondchelation species, said second chelation species including one or morechemical species selected from the group including a first materialincluding said first chelation species, a second material excluding saidfirst chelation species, and combinations thereof, and combinationsthereof wherein, in Formula II, each A is an independently selectedalkali metal Li, Na, or K; and each dopant M may optionally be at leastone independently selected alkaline earth metal Mg or Ca,post-transition metal Al, Ga, In, Sn, or Pb, or transition metal Sc, Ti,V, Cr, Fe, Co, Ni, Cu, Zn, Pd, Ag, or Cd having an average valence j;and Che represents an acid chelating agent which includes ligand bindingatoms that form one or more covalent linkages with Mn or with Mn and M;and wherein 0<j≤4, 0≤k≤0.1, 0≤(p+q)≤6, 0<x≤4, 0<y≤1, 0<z≤1, 0<w≤0.2;−3≤r≤3; 0<v≤0.2; −3≤s≤3; and 0≤n≤6; whereinx+2(y−k)+jk+(m+(r+1)q−6)z+wr+vs=0; and wherein Formula II includes oneor more Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes eachincluding an Mn atom, and wherein p is an average number of NC groupsfound in said one or more Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q)complexes; and wherein q is an average number of Che_I groups found insaid one or more Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; andwherein m is an average valence of said Mn atoms found in said one ormore Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) complexes; wherein (Vac)identifies a Mn(CN)_((6-p-q))(NC)_(p)(Che_I)^(r) _(q) vacancy; whereinCN identifies a cyano group; and wherein NC identifies an isocyanogroup.
 2. The material of claim 1 wherein at least one of said chelationspecies comprises an organic acid.
 3. The material of claim 2 whereinsaid organic acid comprises a compound containing a carboxylate group.4. The material of claim 3 wherein said compound comprises one or moreof acetic acid, formic acid, oxalic acid, gluconic acid, succinic acid,lactic acid, citric acid, sodium glycinate, or sodium oxalate.
 5. Thematerial of claim 1 wherein said organic acid comprises a compoundcontaining an acid of an amine.
 6. The material of claim 5 wherein saidcompound comprises EDTA.
 7. The material of claim 1 wherein said organicacid comprises a compound containing a phosphonic acid group.
 8. Thematerial of claim 7 wherein said compound comprises HEDP.